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A childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12)

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dc.contributor.authorsÇirakoǧlu A., Tarkan-Argüden Y., Devireń A., Kuru D., Yilmaz Ş., Berrak S.G., Canpolat C., Hacihanefioǧlu S.
dc.date.accessioned2022-03-28T14:55:00Z
dc.date.accessioned2026-01-11T17:13:05Z
dc.date.available2022-03-28T14:55:00Z
dc.date.issued2008
dc.description.abstractIt is known that clonal chromosomal changes in childhood ALL are nonrandom and important markers for diagnosis, prognosis and relaps. In this report we present 4 year-old boy with ALL-L1 who has complex chromosomal rearrangements. Chromosome analysis was performed on bone marrow aspiration sample in relaps after one year from diagnosis and induction chemotherapy. The karyotype was; 46,XY,t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12) [11]/46,XY[8] (Turk J Hematol 2006, 25: 152-4).
dc.identifier.issn13007777
dc.identifier.urihttps://hdl.handle.net/11424/256203
dc.language.isoeng
dc.relation.ispartofTurkish Journal of Hematology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAll
dc.subjectChromosome aberrations
dc.subjectCytogenetics
dc.subjectTranslocation
dc.titleA childhood acute lymphoblastic leukemia (ALL) case with t(3;17)(q23;p13),t(5;12)(q31;p13),inv(11)(p15q12)
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage154
oaire.citation.issue3
oaire.citation.startPage152
oaire.citation.titleTurkish Journal of Hematology
oaire.citation.volume25

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